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Oncogenic Transformation by Inhibitor-Sensitive and -Resistant EGFR Mutants
Open accessAbstract
BACKGROUND: Somatic mutations in the kinase domain of the epidermal growth factor receptor tyrosine kinase gene EGFR are common in lung adenocarcinoma. The presence of mutations correlates with tumor sensitivity to the EGFR inhibitors erlotinib and gefitinib, but the transforming potential of specific mutations and their relationship to drug sensitivity have not been described. METHODS AND FINDINGS: Here, we demonstrate that EGFR active site mutants are oncogenic. Mutant EGFR can transform both fibroblasts and lung epithelial cells in the absence of exogenous epidermal growth factor, as evidenced by anchorage-independent growth, focus formation, and tumor formation in immunocompromised mice. Transformation is associated with constitutive autophosphorylation of EGFR, Shc phosphorylation, and STAT pathway activation. Whereas transformation by most EGFR mutants confers on cells sensitivity to erlotinib and gefitinib, transformation by an exon 20 insertion makes cells resistant to these inhibitors but more sensitive to the irreversible inhibitor CL-387,785. CONCLUSION: Oncogenic transformation of cells by different EGFR mutants causes differential sensitivity to gefitinib and erlotinib. Treatment of lung cancers harboring EGFR exon 20 insertions may therefore require the development of alternative kinase inhibition strategies.
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“CL-387785 has also shown potential to overcome T790M mutation-related resistance at the functional level, possibly by effectively inhibiting downstream signaling pathways.”
From Recent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials (2023) · cites this paper as [201]
In the citing paper
“These mutant kinases present a reduced affinity for the ATP, accounting for the increased sensitivity to EGFR TKIs compared with the wild type counterparts, since these inhibitors compete with ATP for binding to the catalytic site [10–12].”
From A decade of EGFR inhibition in EGFR-mutated non small cell lung cancer (NSCLC): Old successes and future perspectives (2015) · cites this paper as [10]
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“Most EGFR exon 20 insertion mutations are 1st generation EGFR-TKIs resistant mutations [15, 18, 19].”
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“Cell culture and transgenic mouse model studies have shown that mutant EGFR has transforming activity (Greulich et al., 2005; Ji et al., 2006; Politi et al., 2006).”
From ERBB Receptors: From Oncogene Discovery to Basic Science to Mechanism-Based Cancer Therapeutics (2014) · cites this paper as Greulich et al., 2005
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Lynch, T. J., Bell, D. W., Sordella, R., Gurubhagavatula, S., Okimoto, R. A., Brannigan, B. W., Harris, P. L., Haserlat, S. M., Supko, J. G., Haluska, F. G., et al. (2004) · New England Journal of Medicine · doi:10.1056/nejmoa040938 · Cited by 11,486
EGFR Mutations in Lung Cancer: Correlation with Clinical Response to Gefitinib Therapy
Paez, J. G., Jänne, P. A., Lee, J. C., Tracy, S., Greulich, H., Gabriel, S., Herman, P., Kaye, F. J., Lindeman, N., Boggon, T. J., et al. (2004) · Science · doi:10.1126/science.1099314 · Cited by 9,368
Self-citationPao, W., Miller, V., Zakowski, M., Doherty, J., Politi, K., Sarkaria, I., Singh, B., Heelan, R., Rusch, V., Fulton, L., et al. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0405220101 · Cited by 4,338
EGFR Mutation and Resistance of Non–Small-Cell Lung Cancer to Gefitinib
Kobayashi, S., Boggon, T. J., Dayaram, T., Jänne, P. A., Kocher, O., Meyerson, M., Johnson, B. E., Eck, M. J., Tenen, D. G., & Halmos, B. (2005) · New England Journal of Medicine · doi:10.1056/nejmoa044238 · Cited by 3,964
Self-citationPao, W., Miller, V. A., Politi, K. A., Riely, G. J., Somwar, R., Zakowski, M. F., Kris, M. G., & Varmus, H. (2005) · PLoS Medicine · doi:10.1371/journal.pmed.0020073 · Cited by 3,527 · cited 1×
“Patients who responded to gefitinib and subsequently relapsed were found to have T790M secondary mutations, also in exon 20 [19,20].”
BackgroundThe ErbB signaling network: receptor heterodimerization in development and cancer
Olayioye, M. A., Neve, R. M., Lane, H. A., & Hynes, N. E. (2000) · The EMBO Journal · doi:10.1093/emboj/19.13.3159 · Cited by 2,489
Shigematsu, H., Lin, L., Takahashi, T., Nomura, M., Suzuki, M., Wistuba, I. I., Fong, K. M., Lee, H., Toyooka, S., Shimizu, N., et al. (2005) · JNCI Journal of the National Cancer Institute · doi:10.1093/jnci/dji055 · Cited by 2,377
Creation of human tumour cells with defined genetic elements
Hahn, W. C., Counter, C. M., Lundberg, A. S., Beijersbergen, R. L., Brooks, M. W., & Weinberg, R. A. (1999) · Nature · doi:10.1038/22780 · Cited by 2,345
Self-citationZhong, Z., Wen, Z., & Darnell, J. E. (1994) · Science · doi:10.1126/science.8140422 · Cited by 2,070
Gefitinib-Sensitizing EGFR Mutations in Lung Cancer Activate Anti-Apoptotic Pathways
Sordella, R., Bell, D. W., Haber, D. A., & Settleman, J. E. (2004) · Science · doi:10.1126/science.1101637 · Cited by 1,605
Flagged first, then by citations
Research works printed but not linked: 2
- Garcia de Palazzo, 1993, Cancer Res, 53, 3217
- Moscatello, 1995, Cancer Res, 55, 5536
Cited by
Sorted by citations
Items 201–300 of 679
Jiang, S., Yamashita, K., Yamamoto, M., Chun-ji, P., Umezawa, A., Saegusa, M., Yoshida, T., Katagiri, M., Masuda, N., Hayakawa, K., et al. (2008) · International Journal of Cancer · doi:10.1002/ijc.23868 · Cited by 75
Tsai, M.-F., Chang, T., Wu, S.-G., Yang, H.-Y., Hsu, Y., Yang, P., & Shih, J. (2015) · Scientific Reports · doi:10.1038/srep13574 · Cited by 75
Sutiman, N., Tan, S. W., Tan, E. H., Lim, W. T., Kanesvaran, R., Ng, Q. S., Jain, A., Ang, M., Tan, W. L., Toh, C., et al. (2016) · Journal of Thoracic Oncology · doi:10.1016/j.jtho.2016.11.2225 · Cited by 75
Na, I. I., Byun, B. H., Kim, K. M., Cheon, G. J., Choe, D. H., Koh, J. S., Lee, D. Y., Ryoo, B., Baek, H., Lim, S. M., et al. (2009) · Lung Cancer · doi:10.1016/j.lungcan.2009.03.010 · Cited by 75
Won, Y., Han, J., Lee, G. K., Park, S.-Y., Lim, K. Y., Yoon, K., Yun, T., Kim, H. T., & Lee, J. S. (2011) · Journal of Clinical Pathology · doi:10.1136/jclinpath-2011-200169 · Cited by 75
Overview of Gefitinib in Non-small Cell Lung Cancer: An Asian Perspective
Jiang, H. (2008) · Japanese Journal of Clinical Oncology · doi:10.1093/jjco/hyn139 · Cited by 74
Current Approaches in NSCLC Targeting K-RAS and EGFR
Aran, V., & Omerović, J. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20225701 · Cited by 74
Genetic and epigenetic changes in lung carcinoma and their clinical implications
Wen, J., Fu, J., Zhang, W., & Guo, M. (2011) · Modern Pathology · doi:10.1038/modpathol.2011.46 · Cited by 77
Cho, J., Pastorino, S., Zeng, Q., Xu, X., Johnson, W. E., VandenBerg, S. R., Verhaak, R. G. W., Cherniack, A. D., Watanabe, H., Dutt, A., et al. (2011) · Cancer Research · doi:10.1158/0008-5472.can-11-0821 · Cited by 73
Self-citationMaity, T. K., Venugopalan, A., Linnoila, I., Cultraro, C. M., Giannakou, A., Nemati, R., Zhang, X., Webster, J. D., Ritt, D., Ghosal, S., et al. (2015) · Cancer Discovery · doi:10.1158/2159-8290.cd-14-0750 · Cited by 73
EGFR is a potential dual molecular target for cancer and Alzheimer’s disease
Choi, H.-J., Jeong, Y. J., Kim, J., & Hoe, H. (2023) · Frontiers in Pharmacology · doi:10.3389/fphar.2023.1238639 · Cited by 72
Advances on EGFR mutation for lung cancer.
Metro, G., & Crinò, L. (2012) · Europe PMC (PubMed Central) · doi:10.3978/j.issn.2218-6751.2011.12.01 · Cited by 73
Pillai, S., Rizwani, W., Li, X., Rawal, B., Nair, S., Schell, M. J., Bepler, G., Haura, E. B., Coppola, D., & Chellappan, S. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.01311-10 · Cited by 72
Minutolo, N. G., Sharma, P., Poussin, M., Shaw, L. C., Brown, D. P., Hollander, E. E., Smole, A., Rodríguez-García, A., Hui, J. Z., Zappala, F., et al. (2020) · Journal of the American Chemical Society · doi:10.1021/jacs.9b11622 · Cited by 73
The CLIP1–LTK fusion is an oncogenic driver in non‐small‐cell lung cancer
Izumi, H., Matsumoto, S., Liu, J., Tanaka, K., Mori, S., Hayashi, K., Kumagai, S., Shibata, Y., Hayashida, T., Watanabe, K., et al. (2021) · Nature · doi:10.1038/s41586-021-04135-5 · Cited by 70
Targeting EGFR in non-small-cell lung cancer: Lessons, experiences, strategies
Stella, G. M., Luisetti, M., Inghilleri, S., Cemmi, F., Scabini, R., Zorzetto, M., & Pozzi, E. (2011) · Respiratory Medicine · doi:10.1016/j.rmed.2011.10.015 · Cited by 73
EGFR inhibition in the treatment of non‐small cell lung cancer
Gerber, D. E. (2008) · Drug Development Research · doi:10.1002/ddr.20268 · Cited by 70
Dokala, A., & Thakur, S. S. (2016) · Oncogene · doi:10.1038/onc.2016.393 · Cited by 70
Tavassoly, O., Sato, T., & Tavassoly, I. (2020) · Molecular Pharmacology · doi:10.1124/mol.120.119909 · Cited by 68
Camorani, S., Crescenzi, E., Colecchia, D., Carpentieri, A., Amoresano, A., Fedele, M., Chiariello, M., & Cerchia, L. (2015) · Oncotarget · doi:10.18632/oncotarget.6066 · Cited by 68
Yoshioka, H., Hotta, K., Kiura, K., Takigawa, N., Hayashi, H., Harita, S., Kuyama, S., Segawa, Y., Kamei, H., Umemura, S., et al. (2010) · Journal of Thoracic Oncology · doi:10.1097/jto.0b013e3181c20063 · Cited by 67
Role of IGF-1 Receptor in Radiation Response
Valenciano, A., Henríquez‐Hernández, L. A., Moreno, M., Lloret, M., & Lara, P. C. (2012) · Translational Oncology · doi:10.1593/tlo.11265 · Cited by 67
Hotta, K., Kiura, K., Toyooka, S., Takigawa, N., Soh, J., Fujiwara, Y., Tabata, M., Date, H., & Tanimoto, M. (2007) · Journal of Thoracic Oncology · doi:10.1097/jto.0b013e318074bc0d · Cited by 67
Toward an early warning system for dengue prevention: modeling climate impact on dengue transmission
Dégallier, N., Favier, C., Menkès, C., Lengaigne, M., Ramalho, W. M., Souza, R., Servain, J., & Boulanger, J. (2009) · Climatic Change · doi:10.1007/s10584-009-9747-3 · Cited by 68
Cooper, W. A., O'Toole, S. A., Boyer, M. J., Horvath, L. G., & Mahar, A. M. (2011) · Pathology · doi:10.1097/pat.0b013e328342629d · Cited by 67
Schneider, M. R., & Yarden, Y. (2015) · Oncogene · doi:10.1038/onc.2015.372 · Cited by 69
EGFR Exon 20 Insertion/Duplication Mutations Characterize Fibrous Hamartoma of Infancy
Park, J. Y., Cohen, C., Lopez, D. D., Ramos, E., Wagenfuehr, J., & Rakheja, D. (2016) · The American Journal of Surgical Pathology · doi:10.1097/pas.0000000000000729 · Cited by 66
Hammerlindl, H., & Schaider, H. (2017) · Journal of Cell Communication and Signaling · doi:10.1007/s12079-017-0435-1 · Cited by 70
Zhong, W., Zhou, Q. H., & Wu, Y.-L. L. C. (2017) · Oncotarget · doi:10.18632/oncotarget.20311 · Cited by 66
Mechanisms of resistance to EGFR targeted therapies
Hrustanovic, G., Lee, B. J., & Bivona, T. G. (2013) · Cancer Biology & Therapy · doi:10.4161/cbt.23627 · Cited by 67
Sharma, S. V., & Settleman, J. E. (2008) · Experimental Cell Research · doi:10.1016/j.yexcr.2008.07.026 · Cited by 67
Degen, M., Natarajan, E., Barron, P., Widlund, H. R., & Rheinwald, J. G. (2012) · American Journal Of Pathology · doi:10.1016/j.ajpath.2012.02.028 · Cited by 64
Lopes, G. L., Vattimo, E. F. D. Q., & de Castro, G. (2015) · Jornal Brasileiro de Pneumologia · doi:10.1590/s1806-37132015000004531 · Cited by 69
Asahina, H., Yamazaki, K., Kinoshita, I., Yokouchi, H., Dosaka-Akita, H., & Nishimura, M. (2006) · Lung Cancer · doi:10.1016/j.lungcan.2006.09.005 · Cited by 63
Impacts of somatic mutations on gene expression: an association perspective
Jia, P., & Zhao, Z. (2016) · Briefings in Bioinformatics · doi:10.1093/bib/bbw037 · Cited by 62
Melese, E. S., Franks, E., Cederberg, R. A., Harbourne, B., Shi, R., Wadsworth, B. J., Collier, J. L., Halvorsen, E. C., Johnson, F. D., Luu, J., et al. (2021) · OncoImmunology · doi:10.1080/2162402x.2021.2010905 · Cited by 62
Selecting Patients for Treatment with Epidermal Growth Factor Tyrosine Kinase Inhibitors
Bonomi, P., Buckingham, L. E., & Coon, J. S. (2007) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-07-0332 · Cited by 62
Epidermal Growth Factor Receptor (EGFR) Signaling and Covalent EGFR Inhibition in Lung Cancer
Heuckmann, J. M., Rauh, D., & Thomas, R. K. (2012) · Journal of Clinical Oncology · doi:10.1200/jco.2012.43.1825 · Cited by 61
HER2 as a target in invasive urothelial carcinoma
Joaquim Bellmunt, B., Werner, L. L., Bamias, A., Fay, A. P., Park, R. S., Riester, M., Selvarajah, S., Barletta, J. A., Berman, D. M., de Muga, S., et al. (2015) · Cancer Medicine · doi:10.1002/cam4.432 · Cited by 61
Role and Relevance of TrkB Mutations and Expression in Non–Small Cell Lung Cancer
Harada, T., Yatabe, Y., Takeshita, M., Koga, T., Yano, T., Wang, Y., & Giaccone, G. (2011) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-10-3034 · Cited by 61
Páez, D. J., GILES, J., McCallum, H. I., Field, H. E., Jordan, D., Peel, A. J., & Plowright, R. K. (2017) · Epidemiology and Infection · doi:10.1017/s0950268817002138 · Cited by 65
The Role of EGFR Inhibition in the Treatment of Non-Small Cell Lung Cancer
Ray, M., Salgia, R., & Vokes, E. E. (2009) · The Oncologist · doi:10.1634/theoncologist.2009-0054 · Cited by 60
Yang, J., Wang, L., Liu, J., Zhong, L., Zheng, R., Xu, Y., Ji, P., Zhang, C., Wang, W., Lin, X., et al. (2012) · Journal of Medicinal Chemistry · doi:10.1021/jm301365e · Cited by 59
Essential roles of mitochondrial and heme function in lung cancer bioenergetics and tumorigenesis
Kalainayakan, S. P., FitzGerald, K. E., Konduri, P. C., Vidal, C., & Li, Z. (2018) · Cell & Bioscience · doi:10.1186/s13578-018-0257-8 · Cited by 59
Landau, M., & Ben‐Tal, N. (2007) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2007.08.001 · Cited by 58
Wu, J., Yu, C., & Shih, J. (2019) · Clinical Lung Cancer · doi:10.1016/j.cllc.2019.06.018 · Cited by 59
Whitsett, T. G., Cheng, E., Inge, L. J., Asrani, K. V., Jameson, N. M., Hostetter, G. H., Weiss, G. J., Kingsley, C. B., Loftus, J. C., Bremner, R. M., et al. (2012) · American Journal Of Pathology · doi:10.1016/j.ajpath.2012.03.026 · Cited by 58
Cooperative Hedgehog-EGFR signaling
Mangelberger, D. (2011) · Frontiers in bioscience · doi:10.2741/3917 · Cited by 57
Lyngaa, R., Nørregaard, K. S., Kristensen, M., Kubale, V., ROSENKILDE, M. M., & Kledal, T. N. (2010) · Oncogene · doi:10.1038/onc.2010.173 · Cited by 57
Epidermal growth factor receptor activation in prostate cancer by three novel missense mutations
Cai, C. Q., Peng, Y., Buckley, M. T., Wei, J., Chen, F. F., Liebes, L., Gerald, W. L., Pincus, M. R., Osman, I., & Lee, P. (2008) · Oncogene · doi:10.1038/sj.onc.1210983 · Cited by 56
Mechanisms of Resistance to EGFR Tyrosine Kinase Inhibitors and Therapeutic Approaches: An Update
Ahsan, A. (2015) · Advances in experimental medicine and biology · doi:10.1007/978-3-319-24223-1_7 · Cited by 56
Inhibition of osimertinib-resistant epidermal growth factor receptor EGFR-T790M/C797S
Lategahn, J., Keul, M., Klövekorn, P., Tumbrink, H. L., Niggenaber, J., Müller, M. P., Hodson, L. E., Flaßhoff, M., Hardick, J., Grabe, T., et al. (2019) · Chemical Science · doi:10.1039/c9sc03445e · Cited by 56
Chung, B., Dimri, M., George, M. E., Reddi, A. L., Chen, G.-S., Band, V., & Band, H. (2009) · Oncogene · doi:10.1038/onc.2009.31 · Cited by 62
Ayoola, A., Barochia, A., Belani, K., & Belani, C. P. (2012) · Cancer Investigation · doi:10.3109/07357907.2012.666691 · Cited by 56
Indazole-Based Covalent Inhibitors To Target Drug-Resistant Epidermal Growth Factor Receptor
Tomassi, S., Lategahn, J., Engel, J., Keul, M., Tumbrink, H. L., Ketzer, J., Mühlenberg, T., Baumann, M., Schultz‐Fademrecht, C., Bauer, S., et al. (2017) · Journal of Medicinal Chemistry · doi:10.1021/acs.jmedchem.6b01626 · Cited by 56
Gefitinib for the treatment of non-small-cell lung cancer
Hida, T., Ogawa, S., Park, J. C., Park, J. Y., Shimizu, J., Horio, Y., & Yoshida, K. (2008) · Expert Review of Anticancer Therapy · doi:10.1586/14737140.9.1.17 · Cited by 58
Naoki, K., Soejima, K., Okamoto, H., Hamamoto, J., Hida, N., Nakachi, I., Yasuda, H., Nakayama, S., Yoda, S., Satomi, R., et al. (2011) · International Journal of Clinical Oncology · doi:10.1007/s10147-011-0187-5 · Cited by 54
TERTPolymorphism rs2736100-C Is Associated with EGFR Mutation–Positive Non–Small Cell Lung Cancer
Wei, R., Cao, L., Pu, H., Wang, H., Zheng, Y., Niu, X., Weng, X., Zhang, H., Favus, M. J., Zhang, L., et al. (2015) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-15-0009 · Cited by 54
Personalized prediction of EGFR mutation-induced drug resistance in lung cancer
Wang, D. D., Zhou, W., Yan, H., Wong, M. P., & Lee, V. H.-F. (2013) · Scientific Reports · doi:10.1038/srep02855 · Cited by 54
Oncogenic transformation and experimental models of human cancer
Anna, C. S. (2007) · Frontiers in bioscience · doi:10.2741/2661 · Cited by 56
Bonine-Summers, A. R., Aakre, M. E., Brown, K. A., Arteaga, C. L., Pietenpol, J. A., Moses, H. L., & Cheng, N. (2007) · Cancer Biology & Therapy · doi:10.4161/cbt.6.4.3851 · Cited by 54
Combined lapatinib and cetuximab enhance cytotoxicity against gefitinib-resistant lung cancer cells
Kim, H., Han, S., Kim, S.-H., Im, S., Oh, D., Bang, Y., & Kim, T. (2008) · Molecular Cancer Therapeutics · doi:10.1158/1535-7163.mct-07-2068 · Cited by 54
Kim, D., Dai, J., Yenwongfai, L. N., Yao, H., Son, Y., Wang, L., Pratheeshkumar, P., Kondo, K., Shi, X., & Zhang, Z. (2014) · Journal of Biological Chemistry · doi:10.1074/jbc.m114.619783 · Cited by 53
The Landscape of EGFR Pathways and Personalized Management of Non-Small-Cell Lung Cancer
Liang Cheng, C., Zhang, S., Alexander, R. E., Yao, Y., MacLennan, G. T., Pan, C.-X., Huang, J., Wang, M., Montironi, R., & Antonio Lopez-beltran, B. (2011) · Future Oncology · doi:10.2217/fon.11.25 · Cited by 53
Masuzawa, K., Yasuda, H., Hamamoto, J., Nukaga, S., Hirano, T., Kawada, I., Naoki, K., Soejima, K., & Betsuyaku, T. (2017) · Oncotarget · doi:10.18632/oncotarget.22297 · Cited by 53
Receptor tyrosine kinases in PI3K signaling: The therapeutic targets in cancer
Jiang, W., & Ji, M. (2019) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2019.03.006 · Cited by 55
Pharmacogenomics of epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors
Jimeno, A., & Hidalgo, M. M. (2006) · Biochimica et Biophysica Acta (BBA) - Reviews on Cancer · doi:10.1016/j.bbcan.2006.08.008 · Cited by 55
Genomic Approaches to Lung Cancer
Thomas, R. K., Weir, B. A., & Meyerson, M. M. (2006) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-06-0098 · Cited by 54
Self-citationSomatic mutations of the epidermal growth factor receptor and non-small-cell lung cancer
Zhang, X., & Chang, A. Y. (2006) · Journal of Medical Genetics · doi:10.1136/jmg.2006.046102 · Cited by 52
Coordinated Targeting of the EGFR Signaling Axis by MicroRNA-27a*
Wu, X., Bhayani, M. K., Dodge, C. T., Nicoloso, M. S., Chen, Y., Yan, X., Adachi, M., Thomas, L., Galer, C. E., Jiffar, T., et al. (2013) · Oncotarget · doi:10.18632/oncotarget.1239 · Cited by 50
Immortalization and malignant transformation of Eukaryotic cells
Stepanenko, A. A., & KAVSAN, V. M. (2012) · Cytology and Genetics · doi:10.3103/s0095452712020041 · Cited by 52
Dutt, A., & Wong, K. (2006) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-06-0414 · Cited by 53
EGF receptor mutations in lung cancer: From humans to mice and maybe back to humans
Arteaga, C. L. (2006) · Cancer Cell · doi:10.1016/j.ccr.2006.05.014 · Cited by 51
Epidermal growth factor receptor inhibitors in the treatment of lung cancer: reality and hopes
Wheatley‐Price, P., & Shepherd, F. A. (2008) · Current Opinion in Oncology · doi:10.1097/cco.0b013e3282f335a3 · Cited by 49
Kancha, R. K., Peschel, C., & Duyster, J. (2011) · Journal of Thoracic Oncology · doi:10.1097/jto.0b013e3182021f3e · Cited by 49
A role of Rab7 in stabilizing EGFR‐Her2 and in sustaining Akt survival signal
Wang, T., Zhang, M., Ma, Z., Guo, K., Tergaonkar, V., Zeng, Q., & Hong, W. (2011) · Journal of Cellular Physiology · doi:10.1002/jcp.23023 · Cited by 49
Ikemura, S., Yasuda, H., Matsumoto, S., Kamada, M., Hamamoto, J., Masuzawa, K., Kobayashi, K., Manabe, T., Arai, D., Nakachi, I., et al. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1819430116 · Cited by 49
EGFR FISH versus mutation: Different tests, different end-points
Cappuzzo, F. (2008) · Lung Cancer · doi:10.1016/j.lungcan.2008.02.008 · Cited by 49
Dixit, A., Torkamani, A., Schork, N. J., & Verkhivker, G. M. (2009) · Biophysical Journal · doi:10.1016/j.bpj.2008.10.041 · Cited by 48
Toschi, L., & Cappuzzo, F. (2007) · The Oncologist · doi:10.1634/theoncologist.12-2-211 · Cited by 48
Uchida, A., Hirano, S., Kitao, H., Ogino, A., Rai, K., Toyooka, S., Takigawa, N., Tabata, M., Takata, M., Kiura, K., et al. (2007) · Cancer Science · doi:10.1111/j.1349-7006.2007.00387.x · Cited by 47
Xu, N., Fang, W., Mu, L., Tang, Y., Gao, L., Ren, S., Cao, D., Zhou, L., Zhang, A., Liu, D., et al. (2015) · Oncotarget · doi:10.18632/oncotarget.6461 · Cited by 48
Design and synthesis of quinazolinones as EGFR inhibitors to overcome EGFR resistance obstacle
Patel, H., Pawara, R. H., Ansari, A., Noolvi, M. N., & Surana, S. J. (2017) · Bioorganic & Medicinal Chemistry · doi:10.1016/j.bmc.2017.03.039 · Cited by 47
EGFR tyrosine kinase inhibitors for the treatment of NSCLC in East Asia: present and future
Yang, C.-H. (2008) · Lung Cancer · doi:10.1016/s0169-5002(08)70102-8 · Cited by 47
Targeting ADAMS and ERBBs in lung cancer
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Metadata
- Authors
- Greulich, H., Chen, T.-H., Feng, W., Jänne, P. A., Alvarez, J. V., Zappaterra, M., Bulmer, S. E., Frank, D. A., Hahn, W. C., Sellers, W. R., & Meyerson, M.
- Affiliations
- Broad Institute (US)
- Brigham and Women's Hospital (US)
- Dana-Farber Cancer Institute (US)
- Corresponding author
- Greulich, Heidi
- Sellers, William R
- Meyerson, Matthew
- ORCID
- Venue
- PLoS Medicine
- Publisher
- Public Library of Science (PLoS)
- Published
- 2005-10-04
- Volume
- 2
- Issue
- 11
- Pages
- e313
- ISSN
- 1549-1277 (ISSN-L)
- 1549-1676
- PMC
- PMC1240052
- OpenAlex
- W2037873277
- Cited by
- 677
- References
- 35
- Citations by year
- 2026: 9 · 2025: 10 · 2024: 10 · 2023: 22 · 2022: 23 · 2021: 23 · 2020: 16 · 2019: 29 · 2018: 20 · 2017: 27 · 2016: 26 · 2015: 47 · 2014: 27 · 2013: 54 · 2012: 46
- FWCI
- 45.72
- Type
- journal article
- Language
- en
- Update notices
- correction (2024-09-16)
- Open access
- gold
- doi.org
- Locations
- PLoS Medicine (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Digital Access to Scholarship at Harvard (DASH) (Harvard University) (submittedVersion, cc-by)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- American Cancer Society
- Doris Duke Charitable Foundation
- Flight Attendant Medical Research Institute
- Barr Foundation
- National Institutes of Health
- National Cancer Institute
- Topics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Treatments and Mutations
- Health Sciences › Medicine › Oncology › HER2/EGFR in Cancer Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer Genomics and Diagnostics
- Keywords
- EGFR mutation, oncogenic transformation, lung adenocarcinoma, erlotinib, gefitinib, EGFR inhibitors, exon 20 insertion, autophosphorylation, Shc phosphorylation, STAT pathway, drug resistance, kinase inhibitors
- MeSH terms
- Erlotinib Hydrochloride, Src Homology 2 Domain-Containing, Transforming Protein 1, Gefitinib, Animals, Antineoplastic Agents, Cell Transformation, Neoplastic, Exons, Humans, Mice, Nude, Mutation, Neoplasms, Experimental, Quinazolines, Transfection, Tumor Stem Cell Assay, Genetic Therapy, Drug Resistance, Neoplasm, NIH 3T3 Cells, Protein Kinase Inhibitors, Adaptor Proteins, Signal Transducing, STAT3 Transcription Factor, Proto-Oncogene Proteins c-akt, Mice, Shc Signaling Adaptor Proteins, ErbB Receptors
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